rs12567232
A SNP on chromosome 1. Its most notable genotype is A;A: Increased risk for Crohn's Disease
- Gene
- None listed
- Location
- Chr 167,262,335 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe
- Minor allele frequency
- 36%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadIncreased risk for Crohn's Disease
- A;GBadIncreased risk for Crohn's Disease
- G;GGoodnormal
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 0% A;G 0% G;G 100%
- European ancestry (Utah)A;A 0% A;G 0% G;G 100%
- Han Chinese (Beijing)A;A 0% A;G 0% G;G 100%
- Japanese (Tokyo)A;A 0% A;G 0% G;G 100%
- Yoruba (Nigeria)A;A 0% A;G 0% G;G 100%
Source and license
Adapted from rs12567232 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.